YM Bio. Com Shs (LSE:YMBA)
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YM BIOSCIENCES Selects Chair for Pivotal Cancer Trial
MISSISSAUGA, ON, March 30 /PRNewswire-FirstCall/ -- YM BioSciences Inc.
(TSX:YM, AIM:YMBA), the cancer drug development company, today announced that
Dr. Kathleen Pritchard, M.D., F.R.C.P.C., hasagreed to act as the North
American Chair for the Company's upcoming international pivotal DEC study in
patients with metastatic breast cancer.
The DEC study is a multinational randomized Phase III clinical trial for YM's
lead drug, tesmilifene, whichwill be combined with epirubicin/cyclophosphamide.
The trial is designed to confirm the survival advantage demonstrated in a
previous Phase III study ("MA19") where tesmilifene was used in combination with
the anthracycline doxorubicin to treat patients with metastatic breast cancer.
In the first Phase III trial, the combination resulted in an overall survival
advantage of greater than 50% over the standard of care alone.
"Dr. Pritchard, of Sunnybrook and Women's College Health Sciences Centre in
Toronto, is an internationally regarded oncologist who will ensure this
important trial is performed under the highest standards," said Mr. David Allan,
Chairman and CEO of YM BioSciences. "With this key step completed, we look
forward to commencing this trial in the coming weeks."
Dr. Pritchard has held leadership roles in a number of national and
international multi-centre clinical trials, is a member of scientific advisory
boards for clinical trials world-wide and is widely published in the major
cancer and general medical journals. Dr. Pritchard holds the following
positions:
- Professor, Departments of Medicine and Public Health Sciences,
University of Toronto
- Chair, Breast Cancer Site Group, Toronto Sunnybrook Regional Cancer
Centre, Sunnybrook & Women's College Health Sciences Centre
- Head, Division of Clinical Trials & Epidemiology, Toronto Sunnybrook
Regional Cancer Centre
About Tesmilifene
Tesmilifene, a small molecule chemopotentiator (for taxanes and anthracyclines),
was originally developed by Dr. L.J. Brandes of the University of Manitoba and
CancerCare Manitoba and licensed by them to YM in 2000. It has previously
completed an international 305-patient Phase III trial in which significant
survival results were demonstrated in women with metastatic breast cancer. The
current Phase III trial is designed to gain approval for the drug. The drug has
been clinically demonstrated to increase the effectiveness of the current
principal chemotherapeutic drugs, anthracyclines and taxanes, which are used in
the majority of cancers.
About YM BioSciences
YM BioSciences Inc. is a cancer drug development company. In addition to
tesmilifene, the Company is developing an EGFr humanized monoclonal antibody
that has completed Phase II trials and a GnRH anti-cancer vaccine also in
clinical trials. YM is also supporting the preclinical development of two
additional cancer products.
Except for historical information, this press release may contain
forward-looking statements, which reflect the Company's current expectation
regarding future events. These forward-looking statements involve risk and
uncertainties, which may cause but are not limited to, changing market
conditions, the successful and timely completion of clinical studies, the
establishment of corporate alliances, the impact of competitive products and
pricing, new product development, uncertainties related to the regulatory
approval process and other risks detailed from time to time inthe Company's
ongoing quarterly and annual reporting.
DATASOURCE: YM BioSciences Inc.
CONTACT: James Smith, The Equicom Group Inc., Tel. +1 (416) 815-0700
x229, Email: ; YM BioSciences Inc., Tel.
+1 (905) 629-9761, Fax +1 (905) 629-4959, Email: